MedPath

Etomidine

Brand Name: Etomidine

Generic Name: Etomidate

Active
Registration Number

DRP-10922

Dosage Form

Emulsion for Injection (I.V.)

Issuance Date

February 8, 2024

Expiry Date

December 17, 2026

Product Information

Philippine FDA product specifications and classification details

Product Specifications

Dosage Strength2 mg/mL
Packaging10 mL USP Type I clear and colorless glass vial with dark gray bromo butyl rubber closure and green flip off seal with embossed 'troikaa' logo in a plastic tray (Box of l's)

Classification

C
Classification
Prescription Drug (Rx)
P
Pharmacologic
General Anesthetic
A
Application
Monitored Release (Reconstruction)/
Philippine FDA Classification

Active Ingredients (1)

Complete list of active ingredients in this pharmaceutical product.

EtomidateActive
Monograph: Etomidate

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

Product

Company

Legal

© 2025 MedPath, Inc. All rights reserved.

MedPath - Medical Intelligence Platform